US20100100124A1

US20100100124A1 - Bioabsorbable surgical composition

Info

Publication number: US20100100124A1
Application number: US12/582,113
Authority: US
Inventors: Allison Calabrese; Walter Skalla
Original assignee: Tyco Healthcare Group LP
Current assignee: Covidien LP
Priority date: 2005-05-05
Filing date: 2009-10-20
Publication date: 2010-04-22
Also published as: AU2010227036A1; EP2314323A2; EP2314323A3; JP2011087931A; CA2718039A1

Abstract

Compounds are provided which can form bioabsorbable compositions useful as adhesives and/or sealants for medical/surgical applications.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is: a continuation-in-part of U.S. application Ser. No. 12/499,146 filed Jul. 8, 2009, which is a continuation-in-part of U.S. patent application Ser. No. 11/123,690, filed May 5, 2005; a continuation-in-part of U.S. application Ser. No. 12/499,141 filed Jul. 8, 2009, which is a continuation-in-part of U.S. patent application Ser. No. 11/123,690, filed May 5, 2005; and a continuation-in-part of U.S. patent application Ser. No. 12/351,492, filed Jan. 9, 2009, which is a continuation-in-part of U.S. patent application Ser. No. 11/123,690, filed May 5, 2005. The entire disclosures of each of the foregoing applications are incorporated by reference herein.

TECHNICAL FIELD

The present disclosure relates to compounds suitable for use in forming bioabsorbable compositions which, in turn, are capable of being used as surgical adhesives or sealants.

RELATED ART

In recent years there has developed increased interest in replacing or augmenting sutures with adhesive bonds. The reasons for this increased interest include: (1) the potential speed with which repair might be accomplished; (2) the ability of a bonding substance to effect complete closure, thus preventing seepage of fluids; and (3) the possibility of forming a bond without excessive deformation of tissue.
Studies in this area, however, have revealed that in order for surgical adhesives to be accepted by surgeons, they must possess a number of properties. They must exhibit high initial tack and an ability to bond rapidly to living tissue; the strength of the bond should be sufficiently high to cause tissue failure before bond failure; the adhesive should form a bridge, typically a permeable flexible bridge; and the adhesive bridge and/or its metabolic products should not cause local histotoxic or carcinogenic effects.
Several materials useful as tissue adhesives or tissue sealants are currently available. One type of adhesive that is currently available is a cyanoacrylate adhesive. However, cyanoacrylate adhesives can have a high flexural modulus which can limit their usefulness. Another type of tissue sealant that is currently available utilizes components derived from bovine and/or human sources. For example, fibrin sealants are available. However, as with any natural material, variability in the material can be observed.
It would be desirable to provide a fully synthetic biological adhesive or sealant that is flexible, biocompatible and highly consistent in its properties. It would also be desirable if the adhesive or sealant was of sufficiently low viscosity to be applied to the desired field.

SUMMARY

Compounds are provided which can form bioabsorbable compositions useful as adhesives and/or sealants for medical/surgical applications. In embodiments, such compositions may be utilized as implants, including patches, for tissue repair. Methods for using such compositions are also provided.
In embodiments, a patch of the present disclosure may include a cured, non-porous film formed from a composition of the present disclosure, and an uncured layer of the composition of the present disclosure applied to a surface of the cured layer.
A method of the present disclosure may include, in embodiments, curing a composition of the present disclosure to form a non-porous film; applying a layer of the composition that is uncured to a surface of the non-porous film; and applying the film to tissue.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 is a graph depicting the strength loss profile of an adhesive of the present disclosure from administration (day 0) through week 4 post-administration; and

FIG. 2 illustrates one embodiment of a two component bioabsorbable composition in combination with a dual syringe applicator.

DETAILED DESCRIPTION

The present disclosure relates to compounds suitable for forming a bioabsorbable composition which may be used as a tissue adhesive or sealant.
The compositions of the present disclosure contain a component that includes an aliphatic diacid linking two dihydroxy compounds (sometimes referred to herein as an “aliphatic polyester macromer”). Up to ten repeats of the aliphatic polyester macromer may be present. The present compounds are not solid at the temperatures encountered in use, but rather are flowable. Flowable materials have a measurable viscosity. For example, the present compounds may have a viscosity of about 1,000 to about 300,000 centipoise (“Cp”) at temperatures of about 0° C. to about 40° C.
Suitable aliphatic diacids which may be utilized in forming the compounds include, for example, aliphatic diacids having from about 2 to about 8 carbon atoms suitable diacids include, but are not limited to sebacic acid, azelaic acid, suberic acid, pimelic acid, adipic acid, glutaric acid, succinic acid, malonic acid, oxalic acid, terephthalic acid, cyclohexyl dicarboxylic acid, fumaric acid, copolymers and combinations thereof.
Suitable dihydroxy compounds which may be utilized include, for example, polyols including polyalkylene oxides, polyvinyl alcohols, and the like. In some embodiments, the dihydroxy compounds can be a polyalkylene oxide such as polyethylene oxide (“PEO”), polypropylene oxide (“PPO”), block or random copolymers of polyethylene oxide (PEO) and polypropylene oxide (PPO).
In one embodiment, a polyethylene glycol (“PEG”) may be utilized as the dihydroxy compound. It may be desirable to utilize a PEG with a molecular weight ranging from about 200 to about 1000, typically from about 400 to about 900. Suitable PEGs are commercially available from a veracity of sources under the designations PEG 200, PEG 400, PEG 600 and PEG 900.
Any method may be used to form the aliphatic polyester macromer. In some embodiments, the aliphatic polyester macromer may be formed by combining adipoyl chloride with a PEG such as PEG 600 and pyridine in a suitable solvent, such as tetrahydrofuran (THF). The solution may be held at a suitable temperature, from about −70° C. to about 25° C., for a period of time ranging from about 4 hours to about 18 hours, after which the reaction mixture is filtered to remove the precipitated pyridine hydrochloride by-product and the resulting aliphatic polyester macromer, here a PEG/adipate compound, may be precipitated from the solution by the addition of ether or petroleum ether, and collected by suitable means which can include filtration. Other methods suitable for making the present compounds will be apparent to those skilled in the art.
Typically, the resulting aliphatic polyester macromer is of the following formula:
HO—(R-A)_n-R—OH
wherein A is a group derived from an aliphatic diacid; R can be the same or different at each occurrence and is a group derived from a dihydroxy compound; and n is 1 to 10. In some useful embodiments, the A group can be derived from adipic acid and R can be derived from a polyethylene glycol having a molecular weight of less then 1,000. The molecular weight and viscosity of these compounds will depend on a number of factors such as the particular diacid used, the particular dihydroxy compound used and the number of repeat units present. Generally, the viscosity of these compounds may be from about 300 to about 10,000 Cp at 25. C and a shear rate of 20.25 s⁻¹.
These compounds are useful for a number of applications. For example, they may be used to produce compounds capable of cross-linking to form a gel matrix that serves as an excellent tissue adhesive or sealant.
For adhesive or sealant applications, it may be desirable to endcap the above aliphatic polyester macromer to provide a reactive end group. Suitable reactive end groups include amine reactive end groups, for example, isocyanate groups, isothiocyanates, diimidazoles, imidoesters, hydroxysuccinimide esters, and aldehydes. Of particular interest are the isocyanate groups. Methods for endcapping the aliphatic polyester macromer to provide a reactive end group are within the purview of those skilled in the art.
For example, the aliphatic polyester macromer may be reacted with an aliphatic or aromatic diisocyanate to produce a diisocyanate-functional compound. Suitable isocyanates for endcapping the aliphatic polyester macromer include aromatic, aliphatic and alicyclic isocyanates. Examples include, but are not limited to, aromatic diisocyanates such as 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, 2,2′-diphenylmethane diisocyanate, 2,4′-diphenylmethane diisocyanate, 4,4′-diphenylmethane diisocyanate, diphenyldimethylmethane diisocyanate, dibenzyl diisocyanate, naphthylene diisocyanate, phenylene diisocyanate, xylylene diisocyanate, 4,4′-oxybis(phenylisocyanate), tetramethylxylylene diisocyanate, tolylenediisocyanate, benzoyl isocyanates, and m-tetramethylxylylenediisocyanate; aliphatic diisocyanates such as tetramethylene diisocyanate, hexamethylene diisocyanate (HMDI), dimethyl diisocyanate, lysine diisocyanate, 2-methylpentane-1,5-diisocyanate, 3-methylpentane-1,5-diisocyanate, 2,2,4-trimethylhexamethylene diisocyanate, and butane diisocyanate; and alicyclic diisocyanates such as isophorone diisocyanate, cyclohexane diisocyanate, hydrogenated xylylene diisocyanate, hydrogenated diphenylmethane diisocyanate, hydrogenated trimethylxylylene diisocyanate, 2,4,6-trimethyl 1,3-phenylene diisocyanate or commercially available DESMODURS® from Bayer Material Science. Other suitable isocyanates include, for example, para-phenylene diisocyanate, p-phenylacetylisocyanate, m-phenylacetylisocyanate, m-phenoxyacetylisocyanate, p-phenoxyacetylisocyanate, and m-hydrocinnamylisocyanate.
Methods for endcapping the aliphatic polyester macromer with a diisocyanate are within the purview of those skilled in the art. For example, the aliphatic polyester macromer may be combined with a suitable diisocyanate, such as toluene diisocyanate, and heated to a suitable temperature ranging from about 55° C. to about 75° C., typically about 65° C. The resulting diisocyanate-functional compound may then be purified by hot extraction with petroleum ether.
The diisocyanate-functional compounds of the present disclosure may be of the following formula:
OCN—X—HNCOO—(R-A)_n-R—OOCNH—X—NCO
wherein X is an aliphatic or aromatic group; A is a group derived from an aliphatic diacid; R can be the same or different at each occurrence and is a group derived from a dihydroxy compound; and n is 1 to 10. In some embodiments, X may be derived from toluene, hexamethylene, tetramethylene, lysine, ethylated lysine isophorone, xylene, diphenylmethane, diphenyldimethylmethane, dibenzyl diisocyanate, oxybis(phenylisocyanate), tetramethylxylylene or optionally mixtures thereof or combinations thereof. The NCO content of the diisocyanate-functional compound can vary from about 3% to about 6%, typically from about 3.5% to about 5%. The viscosity of these diisocyanate-functional compounds will depend on a number of factors such as the particular diisocyanate used, the particular diacid used, the particular dihydroxy compound used and the number of repeat units present. Generally, the viscosity of these compounds may be from about 1,500 to about 50,000 Cp.
It should be understood that more than one different aliphatic polyester macromer can be endcapped in a single reaction. For example, aliphatic polyester macromer of the above-mentioned formula wherein n is 3 can be prepared and combined with aliphatic polyester macromer of the above-mentioned formula wherein n is 5 that had been separately prepared. The mixture of aliphatic polyester macromers can then be endcapped to provide a reactive group in a single reaction. The resulting product will be a mixture of diisocyanate-functional compounds of the formula shown above.
In another aspect of the present disclosure, the functionalized polyester macromer may be further reacted with a multifunctional compound which acts as a branching agent. Suitable branching agents include, for example, polyfunctional acids, anhydrides, alcohols, and mixtures thereof. In some embodiments, the multifunctional compound may be a polyol having 3 to 6 hydroxyl groups, a polycarboxylic acid having 3 to 6 carboxyl groups or a hydroxy acid having a total of 3 to 6 hydroxyl and carboxyl groups.
Representative polyols that may be utilized as the multifunctional compound include glycerol, trimethylol propane, 1,2,4-butanetriol, pentaerythritol, 1,2,6-hexanetriol, sorbitol, 1,1,4,4-tetrakis (hydroxymethyl)cyclohexane, tris(2-hydroxyethyl) isocyanurate, polycaprolactone triol, polylactide triol, polyglycolic acid triol, polydioxanone triol, dipentaerythritol or optionally mixtures thereof. Other multifunctional compounds which may be utilized include triols derived by condensing alkylene oxides having 2 to 3 carbons, such as ethylene oxide and propylene oxide, with polyol initiators. Such multifunctional compounds typically have higher molecular weights ranging from about 400 to about 3000.
Representative polycarboxylic acids that may be used as the multifunctional compound include hemimellitic acid, trimellitic acid, trimesic acid, pyromellitic acid, benzene tetracarboxylic acid, benzophenone tetracarboxylic acid, 1,1,2,2-ethanetetracarboxylic acid, 1,1,2-ethanetricarboxylic acid, 1,3,5-pentanetricarboxylic acid, and 1,2,3,4-cyclopentanetetra-carboxylic acid.
Representative hydroxy acids suitable as the multifunctional compound include malic acid, citric acid, tartaric acid, 3-hydroxyglutaric acid, mucic acid, trihydroxyglutaric acid, and 4-(beta-hydroxyethyl)phthalic acid. Such hydroxy acids contain a combination of 3 or more hydroxyl and carboxyl groups.
Other branching agents suitable for use include, for example, cyclodextrin, trimethylol propane, pentaerythritol, polycaprolactone triol, ethoxylated pentaerythritol, and esters thereof.
In some embodiments, the multifunctional compound may include at least one bioabsorbable group to alter the degradation profile of the resulting branched, functionalized compound. Bioabsorbable groups which may be combined with the multifunctional compound include, for example groups derived from glycolide, glycolic acid, lactide, lactic acid, caprolactone, dioxanone, trimethylene carbonate, and combinations thereof. For example, in one embodiment the multifunctional compound may include trimethylol propane in combination with dioxanone and glycolide. Methods for adding bioabsorbable groups to a multifunctional compound are known. Where the multifunctional compound is modified to include bioabsorbable groups, the bioabsorbable groups may be present in an amount ranging from about 50 percent to about 95 percent of the combined weight of the multifunctional compound and bioabsorbable groups, typically from about 7 percent to about 90 percent of the combined weight of the multifunctional compound and bioabsorbable groups.
The multifunctional compound can have a weight average molecular weight ranging from about 50 to about 5000, typically from about 100 to about 3000, and typically possesses a functionality ranging from about 2 to about 6.
Methods for reacting the multifunctional compound with the functionalized diacid compound are within the purview of those skilled in the art. In some embodiments, the multifunctional compound optionally may be combined with a diisocyanate-functional compound in the presence of a catalyst such as stannous octoate at a temperature ranging from about 50° C. to about 80° C., typically from about 60° C. to about 70° C. for a period of time ranging from about 24 to about 96 hours, typically from about 48 to about 72 hours.
The resulting branched, functionalized compound may thus be of the following formula:
Z—(OCN—X—HNCOO—(R-A)_n-R—OOCNH—X—NCO)_m
wherein Z is a group derived from a multifunctional compound which optionally contains bioabsorbable groups; X is an aliphatic or aromatic group; A is a group derived from an aliphatic diacid; R can be the same or different at each occurrence and is a group derived from a dihydroxy compound; n is 1 to 10; and m is 2 to 6. The viscosity of these branched diisocyanate-functional compounds will depend on a number of factors such as the particular branching agent used, the particular diisocyanate used, the particular diacid used, the particular dihydroxy compound used and the number of repeat units present. Generally, the viscosity of these compounds may be from about 3,000 to about 300,000 Cp at 25° C. and 9.98 s⁻¹shear rate, in some embodiments about 15,000 to about 100,000 Cp at 25° C. and 9.98 s⁻¹shear rate and in yet other embodiments, about 30,000 to about 70,000 Cp at 25° C. and 9.98 s⁻¹shear rate.
As those skilled in the art will appreciate, a mixture of compounds having various degrees of functionality will result from reacting the diisocyanate-functional compound with the multifunctional compound. For example, a single diisocyanate-functional compound may react with the multifunctional compound to provide a compound with a single isocyanate functionality; or two diisocyanate-functional compounds may react with a single multifunctional compound to provide a compound with a two isocyanate functionalities; or three diisocyanate-functional compound may react with a single multifunctional compound to provide a compound with a three isocyanate functionalities; or two multifunctional compound may react with a single diisocyanate-functional compound to provide a compound with no isocyanate functionalities. Those skilled in the art will envision other possible reaction products that may form.
It should be understood that more than one diisocyanate-functional compound can be reacted with a multifunctional compound in a single reaction. For example, aliphatic polyester macromer of the above-mentioned formula wherein n is 3 can be prepared and combined with aliphatic polyester macromer of the above-mentioned formula wherein n is 5 that had been separately prepared. The mixture of aliphatic polyester macromers can then be endcapped to provide a reactive group in a single reaction. The resulting mixture of diisocyanate-functional compounds can then be reacted with a multifunctional compound. As another example, aliphatic polyester macromer of the above-mentioned formula wherein n is 3 can be prepared and endcapped and an aliphatic polyester macromer of the above-mentioned formula wherein n is 5 can be separately prepared and endcapped. The two diisocyanate-functional compounds can then be mixed. The resulting mixture of diisocyanate-functional compounds can then be reacted with a multifunctional compound in a single reaction.
Upon administration to tissue in situ, the functionalized compounds and branched, functionalized compounds described hereinabove cross-link to form a gel matrix that serves as an excellent tissue adhesive or sealant. Normally, the cross-linking reaction is conducted at temperatures ranging from about 20° C. to about 40° C. for a period of time ranging from about fifteen seconds to about 20 minutes or more typically 1 to 10 minutes.
In some embodiments, compositions of the present disclosure may be combined with compounds such as crosslinkers for crosslinking the sealant or adhesive in situ. For example, the crosslinkers may contain amine functional groups, which may react with the isocyanate prepolymer (polyester macromer) to create a crosslinked polyurethane. Suitable crosslinkers include, but are not limited to, amino functional crosslinkers such as ethylene diamine, hexamethylene diamine, lysine, spermine, N-(3-aminopropyl)-1,4-butanediamine, N,N′-bis(3-aminopropyl)-1,4-butanediamine, isomers of hexamethylene diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine, bis-hexamethylene triamine, N,N′-bis(3-aminopropyl)-1,2-ethane diamine, N-3(aminopropyl)-1,3-propane diamine, N-(2-aminoethyl)-1,3 propane diamine, cyclohexane diamine, isomers of cyclohexane diamine, 4,4′-methylene biscyclohexane amine, 4′4′-methylene bis(2-methylcyclohexanamine), toluene diamine, phenylene diamine, isophorone diamine, phenalkylene polyamines, amino-functionalized polyalkylene oxides, polypeptides, and combinations thereof. Crosslinking compositions may be applied to tissue simultaneously with the aliphatic polyester macromers to create a cross-linked sealant or adhesive. In other embodiments, the crosslinking compositions may be used to “pre-treat” a tissue surface, wherein the aliphatic macromer may be later applied to the tissue, crosslinking the composition in situ. Crosslinking compositions may be in a liquid or solid state. The crosslinking compositions may also be combined with various solvents at concentrations from about 0.001% w/w to about 10% w/w, in embodiments from about 0.05% w/w to about 5% w/w. In embodiments, the crosslinking composition is in saline at a concentration of about 0.2% w/w.
The compounds described hereinabove can be used alone or can be formulated into compositions. The concentrations of the components utilized to form the compositions will vary depending upon a number of factors, including the types and molecular weights of the particular components used and the desired end use application of the biocompatible composition, e.g., an adhesive or sealant. Generally, the composition may contain from about 0.5% to about 100% of the previously described functionalized polyester macromer. Where the functionalized polyester macromer has been reacted with a branching agent, the composition may contain from about 0.5 to about 10% of the branching agent by weight.
If the viscosity of the compounds of the present disclosure is deemed too high for a particular application, solutions or emulsions may be formulated that include a solvent in addition to the compounds. Suitable solvents which may be utilized include, for example, polar solvents such as water, ethanol, triethylene glycol, glymes (such as diglyme, triglyme, tetraglyme, and the like), polyethylene glycols, methoxy-polyethylene glycols, dimethylformamide, dimethylacetamide, gamma-butyrolactone, N-methylpyrollidone, ketones such as methyl ethyl ketone, cyclohexanone, diethylene glycol monoethyl ether acetate, diethylene glycol monobutyl ether acetate, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, diethylene glycol monoisobutyl ether, diisobutyl ketone, diacetone alcohol, ethyl amyl ketone, ethyl lactate, and the like, and mixtures thereof. In other embodiments, solvents such as tetrahydrofuran, ethyl acetate, isopropyl acetate, butyl acetate, isopropanol, butanol, acetone, mixtures thereof, and the like, may be utilized.
The amounts of solvent used will depend on a number of factors including the particular reactive compound employed and the intended end use of the composition. Generally, the solvent will be from about 1 to about 50 weight percent of the entire composition. The use of one or more solvents can produce an emulsion having a viscosity of from about 100 to about 1500 Cp. Such emulsions can advantageously be sprayed using any suitable spraying device.
Where the compound includes isocyanate functionality and the solvent contains hydroxyl groups, the solvent is advantageously mixed with the compounds immediately prior to use to avoid undesired pre-gelling.
Compositions in accordance with this disclosure may optionally include one or more catalysts. The addition of a catalyst can decrease the cure time of the compositions of the present disclosure. Catalysts which may be utilized include Lewis acids, tertiary amine catalysts, quaternary amine catalysts, and the like.
Suitable tertiary amine catalysts which may be added include, but are not limited to, triethylenediamine, N-methylmorpholine, pentamethyl diethylenetriamine, dimethylcyclohexylamine, tetramethylethylenediamine, 1-methyl-4-dimethylaminoethyl-piperazine, 3-methoxy-N-dimethyl-propylamine, N-ethylmorpholine, diethylethanolamine, N-cocomorpholine, N,N-dimethyl-N′,N′-dimethylisopropyl-propylene diamine, N,N-diethyl-3-diethyl aminopropylamine and dimethyl-benzyl amine.
Suitable quaternary amine catalysts include, for example, lower alkyl ammonium halides and their derivatives such as hydroxy, chlorhydrin and epoxy substituted lower alkyl trimethylammonium halides such as substituted propyltrimethylammonium chlorides. Quaternary amines which may be utilized include dihydroxypropyltrimethylammonium chloride, chlorohydroxypropyltrimethylammonium chloride, and epoxypropyl-trimethylammonium chloride. Specific examples of the above compounds include 3-chloro-2-hydroxypropyl trimethyl ammonium chloride, 2,3-epoxypropyl trimethyl ammonium chloride, 3-chloro-2-hydroxypropyl trimethyl ammonium chloride, and 2,3-dihydroxypropyltrimethyl ammonium chloride.
In other embodiments, catalysts for use in the cross-linking reaction include 1,4-diazobicyclo [2.2.2] octane, stannous octoate, and the like.
The amount of catalyst employed can range from about 0.5 grams to about 50 grams per kilogram of the compound being cross-linked. In one embodiment, the amount of catalyst ranges from about 0.5 grams to about 10 grams per kilogram of the compound being cross-linked.
Water may also be added to the composition to decrease cure time. When added, water should be introduced at or near the time of use of the composition to avoid unwanted or pre-mature crosslinking. Generally, the amount of water may be from about 1 to about 50 weight percent based on the entire composition. Furthermore, other hydrophilic solutions, including saline and pH buffer solutions, may be combined with the compositions of the present disclosure to decrease cure time.
In certain embodiments, water may be combined with carious catalysts, crosslinkers or other additives such as thickening agents. For example, a two component bioabsorbable composition may include a hydrophilic solvent such as saline as one component, and the second component may include an aliphatic polyester macromer. The hydrophilic solvent may increase the cure time of the bioabsorbable composition. When spraying or applying these two components simultaneously, it may be useful to have similar viscosities of the two components. One way to achieve this may be the addition of thickening agents to the hydrophilic solvent component. Suitable thickening agents include, but are not limited to, polyacrylic acid, poly(sodium acrylate), poly(N-isopropylacrylamide), sodium alginate, guar gum, sodium carboxymethyl guar, cellulose, hydroxyethyl cellulose, carboxymethyl cellulose, konjac glucomannan, oat starch, potato starch, corn starch, xanthan gum, curdlan, various other polysaccharides, and combinations thereof. Thickening agents may be added to a hydrophilic solvent at a concentration from about 0.01% w/w to about 5.0% w/w, in some embodiments from about 1.0% w/w to about 3.0% w/w, and in further embodiments, from about 1.2% w/w to about 2.0% w/w. In one embodiment, the thickening agent is at about 1.5% w/w. Conversely, an additive such as a shear thinning agent may be added to the second polymer component to decrease the viscosity of the second component. Crosslinkers may also be combined with the aqueous phase (to prevent premature gellation of the NCO-functional macromer); suitable crosslinkers include those discussed above.
A variety of optional ingredients may also be added to the bioabsorbable compositions of the present disclosure, including but not limited to surfactants antimicrobial agents, colorants, preservatives, imaging agents e.g., iodine or barium sulfate, or fluorine, or medicinal agents. In some embodiments, the present compositions may optionally contain one or more bioactive agents. The term “bioactive agent,” as used herein, is used in its broadest sense and includes any substance or mixture of substances that have clinical use. Consequently, bioactive agents may or may not have pharmacological activity per se, e.g., a dye. Alternatively a bioactive agent could be any agent which provides a therapeutic or prophylactic effect, a compound that affects or participates in tissue growth, cell growth, cell differentiation, a compound that may be able to invoke a biological action such as an immune response, or could play any other role in one or more biological processes.
Examples of classes of bioactive agents which may be utilized in accordance with the present disclosure include antimicrobials, analgesics, antipyretics, anesthetics, antiepileptics, antihistamines, anti-inflammatories, cardiovascular drugs, diagnostic agents, sympathomimetics, cholinomimetics, antimuscarinics, antispasmodics, hormones, growth factors, muscle relaxants, adrenergic neuron blockers, antineoplastics, immunogenic agents, immunosuppressants, gastrointestinal drugs, diuretics, steroids, lipids, lipopolysaccharides, polysaccharides, and enzymes. It is also intended that combinations of bioactive agents may be used.
Suitable antimicrobial agents which may be included as a bioactive agent in the present compositions include: triclosan, also known as 2,4,4′-trichloro-2′-hydroxydiphenyl ether; chlorhexidine and its salts, including chlorhexidine acetate, chlorhexidine gluconate, chlorhexidine hydrochloride, and chlorhexidine sulfate; silver and its salts, including silver acetate, silver benzoate, silver carbonate, silver citrate, silver iodate, silver iodide, silver lactate, silver laurate, silver nitrate, silver oxide, silver palmitate, silver protein, and silver sulfadiazine; polymyxin; tetracycline; aminoglycosides such as tobramycin and gentamicin; rifampicin; bacitracin; neomycin; chloramphenicol; miconazole; quinolones such as oxolinic acid, norfloxacin, nalidixic acid, pefloxacin, enoxacin and ciprofloxacin; penicillins such as oxacillin and pipracil; nonoxynol 9; fusidic acid; cephalosporins; and combinations thereof. In addition, antimicrobial proteins and peptides such as bovine or rh-lactoferrin and lactoferricin B may be included as a bioactive agent in the present compositions.
Other bioactive agents which may be included as a bioactive agent in the present compositions include: local anesthetics; non-steroidal antifertility agents; parasympathomimetic agents; psychotherapeutic agents; tranquilizers; decongestants; sedative hypnotics; steroids; sulfonamides; sympathomimetic agents; vaccines; vitamins; antimalarials; anti-migraine agents; anti-parkinson agents such as L-dopa; anti-spasmodics; anticholinergic agents (e.g. oxybutynin); antitussives; bronchodilators; cardiovascular agents such as coronary vasodilators and nitroglycerin; alkaloids; analgesics; narcotics such as codeine, dihydrocodeinone, meperidine, morphine and the like; non-narcotics such as salicylates, aspirin, acetaminophen, d-propoxyphene and the like; opioid receptor antagonists such as naltrexone and naloxone; anti-cancer agents; anti-convulsants; anti-emetics; antihistamines; anti-inflammatory agents such as hormonal agents, hydrocortisone, prednisolone, prednisone, non-hormonal agents, allopurinol, indomethacin, phenylbutazone and the like; prostaglandins and cytotoxic drugs; estrogens; antibacterials; antibiotics; anti-fungals; anti-virals; anticoagulants; anticonvulsants; antidepressants; antihistamines; and immunological agents.
Other examples of suitable bioactive agents which may be included in the present compositions include: viruses and cells; peptides; polypeptides and proteins, as well as analogs, muteins, and active fragments thereof; immunoglobulins; antibodies; cytokines (e.g., lymphokines, monokines, chemokines); blood clotting factors; hemopoietic factors; interleukins (IL-2, IL-3, IL-4, IL-6); interferons (β-IFN, (α-IFN and γ-IFN); erythropoietin; nucleases; tumor necrosis factor; colony stimulating factors (e.g., GCSF, GM-CSF, MCSF); insulin; anti-tumor agents and tumor suppressors; blood proteins; gonadotropins (e.g., FSH, LH, CG, etc.); hormones and hormone analogs (e.g., growth hormone); vaccines (e.g., tumoral, bacterial and viral antigens); somatostatin; antigens; blood coagulation factors; growth factors (e.g., nerve growth factor and insulin-like growth factor); protein inhibitors, protein antagonists and protein agonists; nucleic acids such as antisense molecules, DNA, and RNA; oligonucleotides; and ribozymes.
Naturally occurring polymers, including proteins such as collagen and derivatives of various naturally occurring polysaccharides such as glycosaminoglycans, can optionally be incorporated into the compositions as the bioactive agent of the present disclosure.
A single bioactive agent may be utilized to form the present compositions or, in alternate embodiments, any combination of bioactive agents may be utilized to form the present compositions.
Due to the presence of the functionalized compounds and branched, functionalized compounds described hereinabove, the present compositions cross-link to form a gel matrix that serves as an excellent tissue adhesive or sealant. Normally, the cross-linking reaction is conducted at temperatures ranging from about 20° C. to about 40° C. for a period of time ranging from about fifteen seconds to about 20 minutes or more typically 30 seconds to 10 minutes. The exact reaction conditions for achieving cross-linking of the compositions of the present disclosure depend upon a variety of factors, including the functionality of the compound, the degree of endcapping, the degree of functionalization, the presence of a catalyst, the particular solvent, if any, present and the like.
The cross-linked compositions can be used in a medical/surgical capacity in place of, or in combination with, sutures, staples, clamps and the like. In one embodiment, the present compositions can be used to seal or adhere delicate tissue together, such as lung tissue, in place of conventional tools that may cause mechanical stress. The present compositions can also be used to seal air and/or fluid leaks in tissue as well as to prevent post-surgical adhesions and to fill voids and/or defects in tissue.
Where the bioabsorbable composition is intended for delivery of a drug or protein, the amounts of the compounds of the present disclosure can be adjusted to promote the initial retention of the drug or polymer in the bioabsorbable composition and its subsequent release. Methods and means for making such adjustments will be readily apparent to those skilled in the art.
The compositions of the present disclosure can be used for a number of different human and animal medical applications including, but not limited to, wound closure (including surgical incisions and other wounds). Adhesives may be used to bind tissue together either as a replacement of, or as a supplement to, sutures, staples, tapes and/or bandages. Use of the present compositions can eliminate or substantially reduce the number of sutures normally required during current practices, and eliminate the subsequent need for removal of staples and certain types of sutures. The compositions described herein can thus be particularly suitable for use with delicate tissues where sutures, clamps or other conventional tissue closure mechanisms may cause further tissue damage.
To effectuate the joining of two tissue edges, the two edges are approximated, and a composition of the present disclosure is applied to the two approximated edges. The composition crosslinks rapidly, generally taking less than one minute. Compositions of the present disclosure can thus be applied to the wound and allowed to set, thereby closing the wound.
While certain distinctions may be drawn between the usage of the terms “flesh” and “tissue” within the scientific community, the terms are used interchangeably herein as referring to a general substrate upon which those skilled in the art would understand the present bioabsorbable composition to be utilized within the medical field for the treatment of patients. As used herein, “tissue” may include, but is not limited to, skin, bone, neuron, axon, cartilage, blood vessel, cornea, muscle, fascia, brain, prostate, breast, endometrium, lung, pancreas, small intestine, blood, liver, testes, ovaries, cervix, colon, stomach, esophagus, spleen, lymph node, bone marrow, kidney, peripheral blood, embryonic and/or ascite tissue.
The compositions described herein can also be used as sealants. When used as a sealant, a compound of the present disclosure can be used in surgery to form a bioabsorbable composition to prevent or inhibit bleeding or fluid leakage both during and after a surgical procedure. It can also be applied to prevent air leaks associated with pulmonary surgery. Compounds herein may be applied directly to the desired area in at least an amount sufficient to seal off any defect in the tissue and seal off any fluid or air movement. The compositions may also be used to prevent or control blood or other fluid leaks at suture or staple lines.
The present compositions also can be used to attach skin grafts and position tissue flaps during reconstructive surgery. Alternatively, the present compositions can be used to close tissue flaps in periodontal surgery.
Application of the compositions of the present disclosure can be done by any conventional means. These include dripping, brushing, or other direct manipulation of the compositions on the tissue surface, or spraying of the compositions onto the surface. In open surgery, application by hand, forceps or the like is contemplated. In endoscopic surgery, the compositions can be delivered through the cannula of a trocar, and spread at the site by any device known in the art.
In embodiments, a two component bioabsorbable composition may be applied to tissue using a static mixer in combination with a dual syringe. For example, FIG. 2 shows a dual syringe 10, wherein the crosslinking solution, hydrophilic solvent and a thickening agent are in one chamber 12 of the syringe, and the second component including an aliphatic polyester macromer is in the second chamber 14. The plunger 16 may be manually deployed, the components thus exiting the dual syringe 10 and entering static mixer 17. Once in static mixer 17, the two components are contacted and admixed. Once contacted, the two components from the two chambers may crosslink to form a tissue sealant or adhesive 18 within from about 30 seconds to about 10 minutes. The adhesive or sealant should be applied to tissue “t” prior to the two components forming a fully crosslinked system. For example, crosslinking may begin upon exiting the static mixer and complete upon application to tissue “t.” As shown, the dual component syringe 10 is manually pressed, however it is contemplated that other mechanical means including air and gas-assisted sprayers can be used. It is also contemplated that other types of mechanical mixing systems may be used including, for example, a dynamic mixer.
In other embodiments, especially where a composition of the present disclosure is to be utilized as a void filler or sealant to fill a defect in an animal's body, it may be advantageous to more precisely control the conditions and extent of cross-linking. For example, it may be desirable to partially cross-link the composition prior to use to fill a void in animal tissue. In such a case composition of the present disclosure can be applied to the void or defect and allowed to set, thereby filling the void or defect.
In yet other embodiments, the composition of the present disclosure is utilized as a thin polymer film, in conjunction with an adhesive, as a sealant or patch in vivo. The film and adhesive may be formed from the same, or different, composition(s). In embodiments, the film is a cured adhesive formed of the composition of the present disclosure. The film may be cured by moisture in the air, by heat, or other methods within the purview of those skilled in the art. The film may be cast as a thin film in which no bubbles are produced, to form a pore and defect free non-porous layer which prevents or inhibits blood or fluid leakage. In embodiments, the film has a thickness of from about 0.1 mm to about 2 mm, in other embodiments, from about 0.5 mm to about 1 mm. One side of the film is coated with an uncured or partially cured adhesive to be applied to the tissue to be sealed. In embodiments, the adhesive is applied to from about 20% to about 100% of the surface area of a side of the film, in embodiments from about 25% to about 90% of the surface area, and in yet other embodiments from about 40% to about 80% of the surface area. The adhesive may be applied to the film by any conventional means such as those described above.
The patch can be made site specific by cutting the film to any desired shape or size as needed to seal an area of tissue. The film provides strength and has elasticity to support the tissue without run-off of any liquid sealant or adhesive. Accordingly, the patch may be used in a variety of applications including sealing air leaks in the lung, repairing fistulas, sealing anastomoses, as a buttress for suturing friable tissue, etc.
In another embodiment, the present disclosure is directed to a method for using compounds of the present disclosure to adhere a medical device to tissue. The medical device includes an implant. Other medical devices include, but are not limited to, pacemakers, stents, shunts and the like. Generally, for adhering a device to the surface of animal tissue, a composition of the present disclosure can be applied to the device, to the tissue surface or to both. The device and tissue surface are then brought into contact with the present composition therebetween. Once the composition crosslinks and sets, the device and tissue surface are effectively adhered to each other.
The present compositions can also be used to prevent post surgical adhesions. In such an application, a composition of the present disclosure is applied and cured to form a layer on surfaces of internal tissues in order to prevent the formation of adhesions at a surgical site during the healing process.
The resulting bioabsorbable composition has a number of advantageous properties. The bioabsorbable compositions of the present disclosure are safe, possess enhanced adherence to tissue, are biodegradable, have enhanced hemostatic potential, have low cost, and are easy to prepare and use. By varying the selection of the compounds utilized to form the bioabsorbable composition, the strength and elasticity of the bioabsorbable composition can be controlled, as can the gelation time.
The compounds herein rapidly form a compliant gel matrix as the bioabsorbable composition, which insures stationary positioning of tissue edges or implanted medical devices in the desired location and lowers overall required surgical/application time. The resulting bioabsorbable composition exhibits little or no swelling upon gel matrix formation, and therefore retains the positional integrity of the aligned tissue edges and/or location of a medical device. The bioabsorbable composition forms strong cohesive bonds. It exhibits excellent mechanical performance and strength, while retaining the necessary pliability to adhere living tissue. This strength and pliability allows a degree of movement of tissue without shifting the surgical tissue edge.
In order that those skilled in the art may be better able to practice the features of the present disclosure described herein, the following examples are provided to illustrate, but not limit, the features of the present disclosure.

Example 1

91.28 grams of PEG 600 (Sigma Aldrich, St. Louis, Mo.) were added to a clean oven dried and nitrogen cooled (dry herein) 0.5 liter single neck flask. 175 grams (196 ml) of tetrahydrofuran (THF) (J T Baker, Phillipsburg, N.J.) was added to the flask, which dissolved the PEG 600, and then 13.6 grams of anhydrous pyridine (EMD Sciences, Gibbstown, N.J.) were added to the flask. Once dissolved, the solution was added to a dry graduated addition funnel. 19.042 grams of distilled adipoyl chloride (AdCl) (98%, Sigma Aldrich, St. Louis, Mo.) were separately added to a dry one liter, two neck flask, to which 188 grams (211 ml) of THF were then added under static nitrogen.
The flask with the AdCl in THF was chilled in ice for five minutes before the PEG/pyridine/THF solution was added dropwise with stirring set at 500 rpm. The addition of the PEG/pyridine/THF solution proceeded at a rate of 90 drops/minute, with the addition being complete after about 2 hours. Mixing was allowed to continue overnight for about 16 to about 20 hours. The soluble fraction was measured in situ by infrared spectroscopy using a ReactIR 4000 Spectrometer (Mettler-Toledo AutoChem, Columbia, Md.); the ReactIR probe was inserted into one of the necks of the two neck flask; the background utilized was air. The spectrometer scan that was obtained confirmed the presence of PEG/AdCl at a ratio of 3:2.
The resulting material was gravity filtered through filter paper (Scheicher & Schuell #1573, ½) to remove the pyridine hydrochloride salt byproduct. The salt by-product was washed with a small amount of THF at room temperature then filtered again. The filtrate was concentrated on a ROTAVAPOR® rotary evaporator (BÜCHI Labortechnik AG, Flawil, Switzerland). Approximately ¾ of the THF was removed, after which the resulting material was precipitated in 800 ml of anhydrous ethyl ether (Reagent Grade, ACS, 99.0%, VWR International,) stirred at 400 rpm. The mixture was stirred for thirty minutes. The stirring was stopped and the mixture allowed to separate afterwhich the supernatant was and the precipitate transferred to a jar. The product, PEG/adipate at a 3:2 ratio, sometimes referred to herein as dPEG, was vacuum dried overnight.
An additional PEG/adipate was produced using the method described above, but at a ratio of 2:1 (PEG:adipate).

Example 2

Isocyanate endcapping of PEG adipate. A dry 500 ml three neck flask was outfitted with a mechanical stir assembly and dry condenser. The apparatus were setup in a dry room at 2% relative humidity. 57.0 grams of the PEG/adipate produced above in Example 1 was transferred to the flask. 39 grams of toluene diisocyanate (TDI) (technical grade 80%, Sigma Aldrich, St. Louis, Mo.) was added to the flask and the resulting mixture was stirred at 110 rpm and heated to 65° C. while under static nitrogen over night (for 16 to 20 hours). The following day, the temperature was reduced to 60° C., then approximately 150 ml of petroleum ether (ACS Reagent, Sigma Aldrich, St. Louis, Mo.) was added and mixed at 250 rpm for 20 to 30 minutes. The flask was then removed from the heat and the supernatant was decanted. The above process was repeated three times. On the fourth repeat of the process, the solvent was added and stirred for approximately 30 seconds, at which time the supernatant was decanted and the precipitate transferred to a jar (a total of about 60 grams). The material was then vacuum dried at room temperature.
Viscosity was calculated using a Brookfield DV III cone and plate viscosmeter and Rheocalc V2.5 software from Brookfield Engineering Labs, Middleboro, Mass. NCO content was determined by titration on a TitroLine Alpha Autotitrator manufactured by Schott Geräte GmbH, Mainz, Germany using a modification of ASTM D 2572-91. The average NCO content of the material pre-extraction was about 17.9%; the average NCO content of the material post-extraction was about 4.2%. The presence of the NCO endcapped PEG/adipate was confirmed by FTIR and NMR.

Example 3

A degradable branching agent was prepared. To a clean and dry 250 ml three neck flask outfitted with a mechanical stir assembly was added 0.011 grams of stannous octoate (Brand Nu Labs, Meriden Conn.), 8.0 grams of trimethylol propane (TMP) (97% Sigma Aldrich, St. Louis, Mo.), and 30.66 grams of p-dioxanone (US Surgical, Norwalk, Conn.). The mixture was mixed at 50 rpm and placed under static nitrogen overnight. The next morning the reaction mixture was a liquid at 24° C. The reaction mixture was heated to approximately 110° C. for approximately 6 hours, after which 7.0 grams of glycolide (US Surgical, Norwalk, Conn.) was added and temperature was gradually increased to 160° C. After one hour at 160° C., the temperature was reduced to 125° C. for approximately one hour and 15 minutes, after which time the reaction mixture was transferred to a jar and left overnight (about 15 hours).
40 grams of the reaction mixture was then added to a 200 ml single neck flask which, in turn, was heated to 75° C. under vacuum for 24 hours and stirred a rate of 250 rpm. About 26 hours later, the reaction mixture was transferred to a 200 ml single neck flask, and refluxed in ethyl ether while stirring at 200 rpm for 20 minutes. The supernatant was decanted and the refluxing procedure repeated two times to remove residual stannous octoate. The resulting material, a TMP/dioxanone/glycolide branching agent, was transferred to a jar and allowed to dry.

Example 4

The NCO endcapped PEG/adipate of Example 2 was combined with the branching agent of Example 3. 16.59 grams of the NCO endcapped PEG/adipate of Example 2, having an NCO content of 4.2% and a molecular weight of about 3900, was added to a 250 ml three neck flask with a mechanical stir assembly. 0.857 grams of the TMP/dioxanone/glycolide branching agent produced in Example 3 was added to the flask, which was heated to 65° C. while stirring at 50 rpm under static nitrogen. The reaction was allowed to proceed for about 65 hours, at which point the material was transferred to a beaker. The beaker was vacuum dried for one hour then the material was tested for its isocyanate content by titration and found to have an NCO content of about 2.6%.

Example 5

Adhesives utilizing NCO-terminated PEG/adipate prepared according to the procedures set forth above in Example 2 and TMP/dioxanone/glycolide branching agents prepared according to the procedures set forth above in Example 3 were obtained following the procedures described above in Example 4. Additional adhesives were prepared using TMP as a branching agent instead of the branching agents of Example 3. The adhesives that were prepared and their components are summarized below in Table 1. The viscosity was obtained as per the procedures set forth in Example 2 above and NCO content was determined as per the procedures set forth in Example 4 above.
TABLE 1

BASE BRANCHING ADHESIVE

ADHESIVE MATERIAL AGENT VISCOSITY, cP NCO %

A dPEG (3:2) TMP 127,000 3.5

B dPEG (3:2) TMP 42,000 2.8

C dPEG (3:2) dTMP 56,000 2.6

D dPEG (3:2) dTMP 26,000 3.6

E dPEG (3:2) dTMP 59,000 3.0

F dPEG (2:1) TMP 70,000 3.8

The Base Material for Adhesives A-E, dPEG was a PEG600 chain extended with adipoyl chloride at a ratio of 3:2 (PEG600: adipoyl chloride) and TDI; Adhesive F was a PEG600 chain extended with adipoyl chloride at a ratio of 2:1 (PEG600: adipoyl chloride) and TDI. TMP=trimethylolpropane (Aldrich Lot# 10628CA) dTMP=TMP and dioxanone and glycolide. 0.15 grams Bis(hydroxymethyl) propionic acid (BmhP) was added during the branching step in the preparation of Adhesive A.

Example 6

Burst Testing

Staples, adhesives produced above in Example 5, and combinations thereof were subjected to a burst test. The burst test utilized a 25 mm end-to-end anastomosis device (from U.S. Surgical, Norwalk, Conn.) and a test sample of fresh canine colon to test the ability of the adhesives of Example 5 to supplement or replace staples inserted with the end-to-end anastomosis device.
Briefly, the procedure for the burst test was as follows. The anastomotic site of interest was first isolated and a sample was excised. Sufficient tissue was maintained proximal and distal of the staple line (approximately 4 cm each side) to allow the sample to be properly fixtured in a hemostatic clamp. A hypodermic needle was inserted from a syringe pump equipped with a pressure transducer in line into the distal end of the sample and positioned in the clamp with the needle oriented towards the handle of the clamp so that the staple line was centered. The sample was then placed in a triangular test tank, and a sodium fluorescein fluid line was attached to the hypodermic needle. Sodium fluorescein solution was injected into the sample at a rate of 5 cc/min until failure was observed and peak pressure was noted.
Staples only. The anastomosis was performed as per Steichen, et al., (“Mechanical Sutures in Operations on the Small & Large Intestine & Rectum,” Woodbury, Conn.: Ciné-Med, Inc. (2004):72-76), using a 25 mm PPCEEA stapler. The burst pressure test was performed as described above. The burst pressure for the anastomosis sealed only with staples was 0.7 psi-1.3 psi, n=10.
Staples and Adhesive C. The anastomosis was performed as per Steichen et al. using a 25 mm PPCEEA stapler, except that after docking the anvil, but before firing the staples, a bead of Adhesive C (˜0.2 mL) was applied to the tissue on the instrument side approximately between the two rows of staples. After firing, the instrument was removed and the adhesive was allowed to cure for five minutes before performing the burst test. The burst pressure for the anastomosis sealed with the staples and Adhesive C was 1.49 psi-2.1 psi, n=2.
Compromised Anastomosis. Three staples were removed from a 25 mm PPCEEA stapler, two adjacent to the edge of the material, and a third adjacent thereto but closer to the center of the material. The anastomosis was performed as per Steichen et al. using the 25 mm PPCEEA stapler, making sure the compromised portion of the anastomosis was on the anti-mesenteric side of the bowel. The burst pressure for the compromised anastomosis was 0.3 psi, n=10.
Compromised Anastomosis and Adhesive C or Adhesive E. Three staples were removed from a 25 mm PPCEEA stapler, two adjacent to the edge of the material, and a third adjacent thereto but closer to the center of the material. The anastomosis was performed as per Steichen et al. using the 25 mm PPCEEA stapler, except that after docking the anvil, but before firing the staples, a bead of Adhesive C (˜0.2 mL) was applied to the tissue on the instrument side approximately between the two rows of staples. As above, the compromised portion of the anastomosis was on the anti-mesenteric side of the bowel. The instrument was removed and the adhesive was allowed to cure for five minutes before performing the burst test. The burst pressure of Adhesive C in combination with some, but not all, of the staples was 2.1-5.9 psi, n=2.
The same procedure was performed to form a compromised anastomosis, except Adhesive E was utilized instead of Adhesive C. The burst pressure of Adhesive E was 1.12 psi, n=1.
Adhesive E alone with no staples. All staples were removed from a 25 mm PPCEEA. The anastomosis was then performed according to Steichen et al., but before firing the instrument, a bead of Adhesive E (˜0.2 mL) was applied to the tissue on the instrument side approximately between where the two rows of staples would be. Once the instrument was fired, it was opened slightly to reduce the compression on the tissue but it was not opened completely. This was done to keep the ends of the anastomosis together during the five minutes cure time of the adhesive. After five minutes of curing, the anastomosis was tested using the burst test. The burst pressure of Adhesive E was 1.48 psi, n=1.

Example 7

Mesh Pull-Off Testing

The purpose of this example was to mimic hernia repair using a polypropylene mesh with an adhesive. Approximately 0.1 ml of adhesive was placed onto a 16 mm diameter circular piece of mesh with a suture loop through it. The mesh was then placed onto the peritoneum and immediately treated with one drop of saline. After several minutes, the mesh was pulled away from the tissue and the tensile force required to remove the mesh was measured using a Model BG10 premium series force gauge manufactured by Mark-10, Copiague, N.Y. and then recorded. The adhesives utilized, the cure time, pull force (in grams), and observations regarding these tests are set forth below in Table 2.

TABLE 2

		Cure	Pull
		Time	Force
Adhesive	Substrate	min	(grams)	Observations

C	Peritoneum	7	1374	—
C + 10%	Peritoneum	7	920	—
wt/wt
NaHCO₃
C	Peritoneum	2 +	520	Mesh was pulled off at 2 min,
		2.5		placed back down in the
				same place, and pulled again
				after 2.5 more minutes
C	Peritoneum	5	690	Fascia began to separate
				from muscle layer while
				pulling
C	Peritoneum	5	726	Saline was applied once per
				minute after initial
				application
C	Peritoneum	4	700	—

Example 8

Abdominal Aorta Graft

An end-to-side anastomosis was created on the abdominal aorta using an expanded PTFE tubular graft. The graft was sewn on using a 6 pass, interrupted suture. 0.2 mL of Adhesive E was applied through a 16 gauge cannula as a bead around the anastomosis. The adhesive was flushed with saline and let cure for 6 minutes before unclamping the aorta and checking for leaks.
Once the adhesive had been allowed to cure for 6 minutes, the clamps on the aorta were removed to allow complete blood flow past the anastomosis. There were no apparent leaks immediately after the clamps were removed, and even after 10 minutes and manipulation of the graft, there were still no leaks. No bleeding at all was observed through the anastomosis at any time.

Example 9

In Vitro Strength Loss Test

Two rigid foam test blocks were soaked in water prior to application of the adhesive for testing. 0.05 ml of Adhesive B was applied to one testing block using a syringe, the 2^ndtest block mated to the first where the adhesive had been applied, and a 20 gram weight was balanced on top of the construct for 5 minutes. After 1 hour, samples were placed into a glass jar filled with water for 24 hours. The samples were tested for tensile properties using an MTS Sintech 1/G instrument. The first sample was tested by mounting the sample onto the Sintech 1/G using screw action grips and then loaded to failure at 2 in/min to obtain time zero data. The remaining samples were submerged in Sorrenson's buffer and placed into a 37° C. bath for varying time periods of 1 week, two weeks, and four weeks before testing. Tensile data results after 1 week, 2 weeks and 4 weeks in the in vitro bath were obtained as described above with the MTS Sintech 1/G instrument and compared with the time zero data to evaluate strength loss.
The peak loads at failure were recorded for each sample and the strength loss profile is set forth below in Table 3 and accompanying FIG. 1.

TABLE 3

Time	Peak Load [kgf]	St. Dev.	% loss

0	1.79	0.42
1 week	0.84	0.27	53.1
2 weeks	0.64	0.22	23.7
4 weeks	0.24	0.08	61.7
		Total loss	86.3

The material exhibited strength loss after each time period, with the greatest loss occurring after the first week. There was an initial strength of 1.79 kg with an 86% loss in strength after 4 weeks. FIG. 1 is a graph depicting the strength loss profile of the adhesive from administration (day 0) through week 4 post-administration. If strength loss continued along the same trend observed through week 4 (see FIG. 1), total loss in strength could be expected after about 5.24 weeks post-administration.

Example 10

Cytotoxicity Test

The cytotoxicities of Adhesive A and Adhesive F were tested. 1.5 mL of each adhesive was injected directly into a 20 mL MEM solution (Modified Eagle Medium, from Invitrogen Corporation). The cytotoxicity was tested following ISO 10993-5 guidelines. Briefly, the results of the tests are provided on a 5 scale ranking system in which a score of 0, 1, 2, 3, or 4 is obtained. A score of 0 indicates no toxic reaction was observed and a score of 4 indicates a strong toxic reaction was observed. A score of 0, 1, or 2, is considered a non-toxic score, a score of 3 is considered weakly to moderately toxic, and a score of 4 is considered strongly toxic. Scores of 0, 1, or 2 are considered passing scores, that is, the samples do not produce a cytotoxic response.
Adhesive F had a cytotoxicity grade 2, while Adhesive A in combination with BmhP had a cytotoxicity grade 0.

Example 11

Lap Shear Test

Adhesives C, D, and E, were each subjected to a lap shear test. Briefly, room temperature porcine stomach tissue was cut into 15×45 mm pieces using a punch. The tissue was rinsed with saline and blotted to remove excess moisture. 0.1 mL of adhesive was then applied to the end of one of the tissue pieces. The adhesive was spread around to cover an area 15×15 mm at the end of the tissue piece. Another tissue piece was placed on top of the area covered by the adhesive. A 20 gram weight was placed on top of the adhered area for 30 seconds. The weight was removed and the adhesive was allowed to cure for 4.5 minutes more, for a total of 5 minutes cure time. Three separate tissue constructs were prepared, one for each Adhesive C, D and E.
For each tissue construct, the free end of one of the tissue pieces was placed into a grounding clamp, while the free end of the other tissue piece was placed into a second clamp mounted on a counter. A Model BG10 premium series force gauge was attached to the grounding clamp and the force required to pull the pieces apart was recorded.
Adhesive C demonstrated a lap shear of 1100 grams; Adhesive D demonstrated a lap shear of 1262 grams, and Adhesive E demonstrated a lap shear of 1322 grams.

Example 12

A 2:1 molar ratio of PEG 600:adipoyl chloride (MW 183.03) was prepared. PEG 600 (1000.7 grams) was nitrogen dried at 65° C. for 5 hours and reduced to 35° C. for an additional 16 hours. The PEG 600 was then added to a 3 liter jacketed flask reaction with a mechanical stirring assembly, under nitrogen at 20° C., stirring at 400 RPM for at least 10 minutes. Adipoyl chloride (152.6 grams) was added dropwise, at a rate of 60 to 80 drops/minute. The reaction continued at 20° C. for 4 hours, then was increased to 35° C. with bubbling nitrogen for at least 16 hours, after which the reaction temperature was decreased to 25° C. Approximately 750 grams of the material was dissolved in 2 liters of THF and transferred to a 4 liter Erlenmeyer flask. Aluminum oxide (650 grams) was added and stirred for 1 hour before decanting and pressure filtering (using paper with 0.45 μm pores). The PEG adipate was then attached to a ROTOVAPOR® and then ethyl ether was added (to remove excess THF). The concentrated THF solution was then precipitated in the ether with mixing and the ether was decanted after about 30 minutes and 1 liter of fresh ethyl ether was added. The material was mixed again and the ether decanted. The material (PEG adipate) was then stirred for an additional 30 minutes, decanted, and transferred to a glass jar under vacuum. The PEG adipate was endcapped with isocyanates, using a method similar to the one described in Example 2 above, with the primary difference being 112 grams of PEG adipate was added to 43 grams of TDI. The reaction was stirred under static nitrogen for up to 6 hours. Once reacted with petroleum ether, the supernatant was decanted ten times. The NCO content of the material post-extraction was about 4.1%. The material was branched using TMP as the branching agent.

Example 13

Lap Shear Test

Ten dual syringes (with static mixer) were loaded with about 1.5 ml of the material of Example 12 (herein referred to as Adhesive H) in one syringe barrel and 1.5 ml of 0.2% Bis (3-aminopropyl) amine in saline in the other syringe barrel. Another ten dual syringes were loaded with about 1.5 ml of Adhesive H in one barrel and 1.5 ml of 0.2% Bis (3-aminopropyl) amine in a 1.5% solution of Carboxymethyl cellulose in saline in the other single barrel. Samples were manually dispensed using a 2.5″, 16 element static mixer. Each of the samples from the syringes was subjected to the lap shear test of Example 11. Results are summarized in Table 4 below.

TABLE 4

Samples	CMC (g)	No CMC (g)

1	1596	1276
2	1522	1292
3	1604	1446
4	1656	1346
5	1562	1238
6	1354	1764
7	1942	1266
8	1666	750
9	1540	1860
10	1846	1622
average	1628.8	1386
standard	166.1	314.5
deviation

Example 14

Adhesives utilizing 55.01 grams of NCO-terminated PEG/adipate having an NCO content of about 4.411% to about 4.406%, prepared according to the procedures set forth above in Example 2, and 0.640 grams of a TMP branching agent prepared according to the procedures set forth above in Example 5, were combined according to the procedures set forth above in Example 5. The adhesives had 8.75 mole % TMP and viscosities ranging from about 33,566.40 cP to about 34,809.60 cP.
The adhesives were packaged in 4×10 cc syringes and subjected to the lap shear test of Example 11. A lap shear of 1060 grams at about 5 minutes was observed during a first test trial. A second trial demonstrated a lap shear of 1654 grams at 5.75 minutes and a third trial demonstrated a lap shear of 970 grams at 4 minutes.

Example 15

A clean 1 liter 2-neck flask and a 12″ reflux condenser, with inner coil and inner wall, were rinsed with deionized water and placed in an oven to dry. Upon removal from the oven, the pieces were setup and flame dried. A twin connecting hose adapter was placed on the top of the condenser so that the heating and cooling process were completed under nitrogen. The nitrogen ran through a DRIERITE gas drying unit (W. A. Hammond Drierite Co. LTD., Stock No. 26800).
In a first reaction stage, polycaprolactone triol was added to an oven dried, nitrogen cooled 100 ml round bottom flask. Approximately 70 ml of warm THF was added. The 100 ml round bottom flask was shaken, checked for clarity, and added to the 1 liter flask.
Approximately 130 ml of warm THF was added to an oven dried, nitrogen cooled 200 ml round bottom flask. HMDI was added to the THF. The 200 ml round bottom flask was then shaken, checked for clarity, and added to the 1 liter flask.
A total of 200 ml of THF was added to the 1 liter flask, resulting in a 5% component to solvent ratio. The solution was rapidly stirred as the solution was cooled under static nitrogen overnight.
Triethylamine, dried under molecular sieves, was added via pipet and reflux began for about 4.5 hours.
In a second reaction stage, PEG 600 was added to an oven dried, nitrogen cooled 200 ml round bottom flask. Approximately 160 ml of warm THF was added and the 200 ml round bottom flask was shaken, checked for clarity, and added to the 1 liter flask.
60 ml of warm THF was added to an oven dried, nitrogen cooled 100 ml round bottom flask. HMDI was added to the THF. The 100 ml round bottom flask was shaken, checked for clarity, and added to the 1 liter flask. The 100 ml round bottom flask was then rinsed with an additional 40 ml of THF and added to the 1 liter flask. Reflux began for about 4.75 hours.
A total of 460 ml THF (200 ml THF added from stage 1 and 260 ml THF added from stage 2) resulting in approximately a 9% solution. The solution was allowed to cool overnight under static nitrogen with mixing to form a clear solution when cooled.
The components utilized are summarized below in Table 5.

TABLE 5

	Molecular
Component	Weight	Mole	Gram	Mole Ratio

STAGE

1
Polycaprolactone triol	300	0.0120	3.60	1.0
(Aldrich Lot # 01101MZ-
refluxed in toluene and
dried under vacuum)
1,6	168	0.0380	6.39	3.17
Diioscyanatohexane
(Aldrich Lot # 07617DA)
Triethylamine	107	1.75E−3	0.25	0.15
(Aldrich Lot # 06615BA)
STAGE 2
Poly(ethylene glycol)	600	0.0359	21.57	3.00
(Aldrich Lot # 11258EB)
1,6	168	0.0529	8.89	4.41
Diisocyanatohexane
(Aldrich Lot # 07617DA)

Example 16

The components of the composition of Example 15 were prepared and combined according to the procedures set forth above in Example 15, except that the amounts of THF utilized were different. 40 ml and 50 ml, respectively, of warm THF were utilized in stage 1 for a total of 90 ml of THF added, resulting in a 6% component to solvent ratio. In stage 2, 75 ml and 100 ml of warm THF were utilized for an overall total of 265 ml THF, forming approximately a 7% solution. The components utilized are presented in the table below:

TABLE 6

	Molecular
Component	Weight	Mole	Gram	Mole Ratio

STAGE

1
Polycaprolactone triol	300	0.00492	1.477	1.0
(Aldrich Lot # 01101MZ-
refluxed in toluene and
dried under vacuum)
1,3 Bis(1-isocyanto-1-	244	0.0158	3.857	3.21
methylethyl) benzene
(Aldrich Lot # 11018HB)
Triethyamline	107	2.34E−3	0.25	0.47
(Aldrich Lot # 06615BA)
STAGE 2
Poly(ethylene glycol)	600	0.01475	8.85	3.00
(Aldrich Lot # 11258EB)
1,6 Diisocyantohexane	168	0.0214	3.60	4.36
(Aldrich, Lot # 07617DA)

Example 17

An NCO-terminated PEG/adipate was prepared at a ratio of 4:3 according to the procedures set forth above in Example 1, and a pentaerythriltol branching agent was combined with the PEG-adipate to prepare an adhesive utilizing the procedures described above in Example 5. 15.41 grams of dPEG(4:3) with an NCO content of 4.7% was combined with 0.1376 grams of pentaerythritol to produce an adhesive having a viscosity of about 51,513.10 cP and an NCO content of 3.1%.

Example 18

An NCO-terminated PEG/adipate was prepared at a ratio of 2:1 according to the procedures set forth above in Example 1. Various branching agents were combined with the PEG/adipate to prepare adhesives utilizing the procedures described above in Example 5, as illustrated in the table below:

TABLE 7

BASE MATERIAL	BRANCHING AGENT

129.20 grams of dPEG(2:1)	64.59 grams of 4,4-methylene
	bis(phenyl isocyanate)
115 grams of dPEG(2:1)	44 grams of toluene diisocyanate
35.26 grams of dPEG(2:1)	18.04 grams of lysine diisocyanate
111.31 grams of dPEG(2:1)	32.9 grams of 1,4 phenylene diisocyanate

Example 19

An adhesive utilizing 85.51 grams of NCO-terminated PEG/adipate prepared according to the procedures set forth above in Example 2 was removed from vacuum and added to a clean dry 250 ml 3-neck flask. About 0.01051 grams of 4-dimethylaminopyridine flakes were added to the PEG/adipate, followed by 38.45 grams of HMDI. The components were placed under static nitrogen and mixed for about 5½ hours at about 65° C. The temperature was decreased to about 60° C. and washed multiple times for about 3-5 minutes with from about 100 to about 150 ml of petroleum ether. After the final wash, the resulting polymeric material was decanted and vacuum dried. The percent isocyanate in the polymeric product, found via titration, was about 4.39%.
About 1.29 grams of TMP was added to about 97.5 grams of the vacuum dried polymer. The polymer in TMP was mixed for about 23 hours at 65° C. at about 50 revolutions per minute (rpm). The mixture was then added to 3 ml syringes and packaged in individual foil bags. About 0.37 grams of vitamin E was added to the remaining 35.2 grams of TMP branched polymer, and mixed for about 80 minutes at 65° C. under static nitrogen at 50 rpm. The mixture was added to 3 ml syringes and packaged in individual foil bags.

Example 20

128 grams of glycolide, 103 grams of s-caprolactone, and 7.6 grams of propylene glycol were added to a clean, dry 1 liter reactor flask and dried with nitrogen overnight. The flask was heated to 150° C. and the agitator was set to 120 RPM. When the mixture reached 150° C., 0.16 grams of Sn(Oct)₂was added. The mixture was allowed to react at 150° C. for 24 hours and the agitator adjusted as necessary.
The mixture was then cooled to 130° C. 600 grams of PEG 600 and 0.28 grams of Sn(Oct)₂was added to the mixture. The agitator speed was set to 120 RPM and the mixture reacted for 5 hours. Upon completion, the mixture was poured into glass jars.

Example 21

50.33 grams of the polymer produced in Example 20 was added to a 250 ml round bottom flask with 49.67 grams of PEG 900, and blanketed with nitrogen. An oil bath was set to 155° C. and 0.04 grams of stannous octoate was added. The reaction was allowed to proceed at 155° C. for 4 hours.
The mixture was cooled to 120° C. and 100 grams of HMDI was added. The mixture was agitated at 120° C. for 24 hours.
The mixture was then washed in petroleum ether and dried under vacuum.

Example 22

NCO-terminated PEG/adipate was prepared from the materials set forth below:

TABLE 8

			MOLAR
MATERIAL	MASS (g)	MOLES	RATIO

PEG 600 - (MW 600)	959.1	1.6	2.0
(S.A. Part # 202401, lot # 01828BH)
Adipoyl Chloride - (MW 183.03)	146.2	0.8	1.0
(S.A. Part # 165212, lot # 04705LE)

The general synthesis was as follows. To a clean, dry 3 liter 4-neck jacketed reaction flask with mechanical stirring assembly (stir blade and PTFE turbine), nitrogen blanket, and a JULABO circulating bath at 65° C. attached to the jacket for temperature control, were added the PEG via a vacuum adapter and equilibrated at about 65° C. with stirring at 400 RPM. The PEG was dried by bubbling nitrogen through the material overnight using Teflon tubing or a pipette.
The jacket temperature was decreased to 20° C. and the adipoyl chloride was weighed out into a clean, dry 250 ml addition funnel. The adipoyl chloride funnel was attached to the reactor via an offset adapter and added at a rate of about 60-80 drops/minute until all the adipoyl chloride was added. The jacket temperature remained at 20° C. for 2.5 hours and was then increased to 45° C. overnight with nitrogen bubbling through the material.
The jacket temperature was decreased to 20° C. and 1.5 liter THF was added to the reactor and stirred until dissolved for at least 10 minutes. The solution was transferred to a clean 4 liter Erlenmeyer flask and an additional 0.5 liter THF was added.
A purification system was set-up including an alumina filled column filled with neutral alumina having a mass of 1,235 grams and THF. The solution was pumped through the column at a rate of 60-70 ml/min. After all the solution entered the column, 1 liter of fresh THF was pumped through the column. A ROTOVAPOR® was utilized to filter the solution down to about 1 liter total. About 600 ml of diethyl ether was added to the solution and shaken vigorously. The ether was decanted, repeated, and decanted again. The solution was then placed back on the ROTOVAPOR® to remove remaining ether before transferring the product to glass jars to dry under vacuum.
1,4 phenylene diisocyanate was purified by adding 33.3 grams of 1,4 phenylene diisocyanate to a 500 ml single neck flask. 255 grams of toluene was added to the flask with a magnetic stir bar. A clean vigreaux column was added to the flask and a static nitrogen line was added to the top of the column. The flask was placed in a 50° C. bath for 3 hours and then filtered through a paper filter. The solution was then placed back on the ROTOVAPOR® at 35 torr with the bath temp at from about 45 to about 50° C. until dry. The product was washed 3 times with about 150 ml petroleum ether. The resulting white solids obtained were transferred to a jar and vacuum dried overnight.
To a 250 ml 3-neck flask, 15.362 grams of the purified 1,4 phenylene diisocyanate was added, followed by 80.067 grams of the PEG/adipate. The components were placed under static nitrogen and set to 70° C. in an oil bath. The components were mixed for 2 hours at 70° C. at 100-150 RPM. The temperature was increased to 75° C. for an additional two hours. The flask was then removed from the bath with continued mixing. The NCO content of the composition was 4.303%.
Any NCO which had sublimed to the neck of the flask was removed with an ethanol dampened wipe and placed on a balance; 88.695 grams remained in the flask. To the 88.695 grams, 0.5544 grams of TMP was added which had been dried and stored in a dry room. The composition was then sealed under static nitrogen and added to a bath at 65° C. overnight. The temperature was decreased to 40° C. and moved to a dry room when the oil bath reached 45° C. The composition was then transferred to 3×30 cc syringes.

Example 23

A thin layer of the composition of Example 20 was cast on a glass surface (approximately 0.05 mm) and allowed to cure overnight to form a film. A small piece of the film was cut and one side was coated with a thin layer of the composition, with excess composition removed by pressing the film down on a Teflon sheet. The coated film was applied to porcine stomach and left to cure for 5 minutes.

Example 24

The coated film of Example 23 was pre-swelled prior to placement on the porcine stomach.
It will be understood that various modifications may be made to the embodiments disclosed herein. For example, the diisocyanate functionalized aliphatic polyester macromer can be used to prepare polyurethanes and used for applications other than adhesives or sealants. As another example, the branched diisocyanate functionalized aliphatic polyester macromer can be cross-linked and molded into solid articles useful in a variety of applications, including but not limited to solid, biodegradable implants. Therefore the above description should not be construed as limiting, but merely as exemplifications of preferred embodiments. Those skilled in the art will envision other modifications within the scope and spirit of the claims appended hereto.

Claims

1. A patch comprising:

a cured, non-porous film comprising a composition; and

an uncured layer of the composition applied to a surface of the cured layer.

2. The patch according to claim 1, wherein the composition includes an aliphatic polyester macromer.

3. The patch according to claim 2, wherein the aliphatic polyester macromer is a compound of the formula:

HO—(R-A)_n-R—OH

wherein A is a group derived from an aliphatic diacid; R can be the same or different at each occurrence and is a group derived from a dihydroxy compound having a molecular weight less than 1,000; and n is 2 to 10.

4. The patch according to claim 2, wherein the aliphatic polyester macromer is endcapped with reactive end groups.

5. The patch according to claim 4, wherein the composition includes a compound of the formula:

OCN—X—HNCOO—(R-A)_n-ROOCNH—X—NCO

wherein X is an aliphatic or aromatic group; A is a group derived from an aliphatic diacid; R can be the same or different at each occurrence and is a group derived from a dihydroxy compound; and n is 1 to 10.

6. The patch according to claim 2, wherein the aliphatic polyester macromer is functionalized with a branching agent.

7. The patch according to claim 6, wherein the composition includes a compound of the formula:

Z—(OOCNH—X—NHCOO—(R-A)_nR—OOCNH—X—NCO)_m

wherein Z is a group derived from a multifunctional compound; X is an aliphatic or aromatic group; A is a group derived from an aliphatic diacid; R can be the same or different at each occurrence and is a group derived from a dihydroxy compound; n is 1 to 10; and m is 2 to 6.

8. The patch according to claim 1, wherein the composition includes crosslinkers.

9. The patch according to claim 1, wherein the composition includes a catalyst.

10. The patch according to claim 1, wherein the composition includes a hydrophilic solvent.

11. The patch according to claim 1, wherein the composition includes a bioactive agent.

12. The patch according to claim 1, wherein the cured layer is about 0.01 mm to about 1 mm thick.

13. The patch according to claim 1, wherein the uncured layer of the composition covers between about 20% to about 100% of the surface of the cured layer.

14. A method comprising:

curing a composition to form a non-porous film;

applying a layer of the composition that is uncured to a surface of the non-porous film; and

applying the film to tissue.

15. The method according to claim 14, further comprising:

reacting at least one aliphatic polyester macromer of the formula:

HO—(R-A)_n-R—OH

wherein A is a group derived from an aliphatic diacid; R can be the same or different at each occurrence and is a group derived from a dihydroxy compound having a molecular weight less than 1,000; and n is 1 to 10 with at least one diisocyanate to provide at least one diisocyanate-endcapped macromer; and

reacting the at least one diisocyanate-endcapped macromer with at least one multifunctional compound to provide the composition.

16. The method according to claim 15, wherein two different aliphatic polyester macromers are reacted with at least one diisocyanate in a single reaction to provide a mixture of diisocyanate-endcapped macromers, and the mixture of diisocyanate-endcapped macromers is reacted with a multifunctional compound in a single reaction to provide the composition.